氘可来昔替尼片 | China Drugs ListDeucravacitinib tablets | China Drugs List

本页为公开参考信息,不构成医疗建议、处方或药品供应要约。请向持证专业人士确认当前批准情况、可获得性及适用性。

企业
Bristol-Myers SquibbPharma EEIGBristol-Myers Squibb Pharma EEIG
药品类型
化学药Chemical medicine
治疗领域
皮肤科Dermatology
公开来源记录的适应症
(1)适合系统治疗或光疗的中重度斑块状银屑病成人患者;(2)既往改善病情抗风湿药(DMARD)应答不佳或不耐受的活动性银屑病关节炎成人患者。1. Adults with moderate-to-severe plaque psoriasis who are candidates for systemic therapy or phototherapy. 2. Adults with active psoriatic arthritis who responded inadequately to, or could not tolerate, a disease-modifying antirheumatic drug (DMARD).
适应症来源与口径
来源日期: 2026-06-15. 新增适应症可能由较新的公告或申报资料支持,而非旧版完整说明书;请查看适应症来源。Source date(s): 2026-06-15. Additional indications may be supported by newer announcements or submissions rather than the older full label; see the indication sources.
说明书信息局限
已找到官方药品说明书链接;尚未核实文件正文。Official prescribing-information link located; the document body has not yet been verified.
中国可获得性状态
已核实中国历史批准记录;尚未逐项核查每个产品目前是否持续上市销售。Historical Chinese approval verified; current continuous market availability has not been checked for every product.
海外状态
日本, 英国: 已取得当地获批/上市公告及官方价格来源。每条价格记录注明适应症与日期;未全面核查其他市场。Japan, United Kingdom: local approval / launch announcements and official price sources obtained. Indications and dates are specified in each price record; other markets not exhaustively reviewed.
医保分类
已纳入国家医保(乙类)Included in national insurance (Category B)
医保版本
2025版;2026年1月1日起执行2025 edition; effective 1 January 2026
医保限制
限适合系统治疗或光疗的成年中重度斑块状银屑病患者。Limited to adults with moderate-to-severe plaque psoriasis who are candidates for systemic therapy or phototherapy.
医保期限
2025-01-01 至 2026-12-312025-01-01 to 2026-12-31
医保核查说明
按成分/剂型名称精确或标准化匹配。报销仍取决于剂型及目录所列支付限制。Matched by exact or normalized ingredient/formulation name. Reimbursement still depends on the dosage form and listed payment restrictions.

来源

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